Since its creation in 2003, Anteis has developed various ranges of hyaluronic acid
gel-based medical devices in several areas such as aesthetic dermatology,
ophthalmology and orthopaedics.
Anteis offers CE mark products only, and in the medical device field, a product CE mark guarantees compliance with the European directive 93/42/EEC, which
means, among others:
- an analysis of risk, safety evidenve
- a quality and manufacturing system conforming to current standards
- a product-tracking system in case of recall.
In addition to these standards, Anteis has made a commitment to investing in studies providing clinical evidence of patient benefit and practitioner satisfaction. Our vision is to become the leading innovative company based on modified/functionalized biopolymers for injection treatment.
So the creation of a clinical research pole allows Anteis to be even closer to doctors and their patients by developing innovative treatments, methods and products that meet their real expectations, wishes and needs. Efficacy, safety and user-friendliness are scientifically tested as part of these clinical studies.
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